Back to Search
JOSEPH ZEMAN, MD
MD
Pulmonary Disease Physician
NPI: 1831351659Individual
Specialties, Licenses & Credentials
Pulmonary Disease PhysicianPrimary
Internal Medicine — Pulmonary Disease
Code: 207RP1001X
0101247507(VA)
Research & Publications (20)
Enzyme replacement therapy for Gaucher disease in twin pregnancy.
PMID 19349046·Int J Gynaecol Obstet·2009
5-case
Mucopolysaccharidosis type I in 21 Czech and Slovak patients: mutation analysis suggests a functional importance of C-terminus of the IDUA protein.
PMID 19396826·Am J Med Genet A·2009
8-other
TMEM70 protein - a novel ancillary factor of mammalian ATP synthase.
PMID 19103153·Biochim Biophys Acta·2009
7-preclinical
Common and specific emotion-related predictors of anxious and depressive symptoms in youth.
PMID 19039662·Child Psychiatry Hum Dev·2009
8-other
Loss of function of Sco1 and its interaction with cytochrome c oxidase.
PMID 19295170·Am J Physiol Cell Physiol·2009
8-other
Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency.
PMID 18221507·BMC Genomics·2008
4-observational
The impact of mitochondrial tRNA mutations on the amount of ATP synthase differs in the brain compared to other tissues.
PMID 18319067·Biochim Biophys Acta·2008
5-case
Activities of respiratory chain complexes and pyruvate dehydrogenase in isolated muscle mitochondria in premature neonates.
PMID 17698302·Early Hum Dev·2008
4-observational
Structural analysis of tissues affected by cytochrome C oxidase deficiency due to mutations in the SCO2 gene.
PMID 18254779·APMIS·2008
8-other
The influence of temperature and hydration on the sorption properties of bentonite.
PMID 18155330·J Environ Radioact·2008
8-other
1H MR spectroscopy as a diagnostic tool for cerebral creatine deficiency.
PMID 18726626·MAGMA·2008
5-case
TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy.
PMID 18953340·Nat Genet·2008
8-other
The developmental changes in mitochondrial DNA content per cell in human cord blood leukocytes during gestation.
PMID 18052680·Physiol Res·2008
8-other
[Long-term results of calcaneal fracture treatment by open reduction and internal fixation using a calcaneal locking compression plate from an extended lateral approach].
PMID 19150004·Acta Chir Orthop Traumatol Cech·2008
8-other
Prolonged impairment of polymorphonuclear cells functions in one infant with transient zinc deficiency: a case report.
PMID 19548600·Prague Med Rep·2008
5-case
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy.
PMID 18038146·Eur J Pediatr·2008
6-review
A new mutation within the porphobilinogen deaminase gene leading to a truncated protein as a cause of acute intermittent porphyria in an extended Indian family.
PMID 18070416·Folia Biol (Praha)·2007
8-other
Knockdown of human Oxa1l impairs the biogenesis of F1Fo-ATP synthase and NADH:ubiquinone oxidoreductase.
PMID 17936786·J Mol Biol·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- NATIONAL NAVAL MEDICAL CENTER 8901 WISCONSIN AVE, GRADUATE MEDICAL EDUCATION BLDG 10 RM 1006
BETHESDA, MD 20889 - Phone
- (301) 319-8278
Quick Facts
- NPI
- 1831351659
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile